A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037045



Internal ID21946388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92798183..92798236hg38UCSC Ensembl
chr14:93264528..93264581hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609932
Samples
Known GenesGOLGA5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037045
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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